On completing your regulatory documentation, our medical communications (med comms) specialists can engage with your trial data to communicate your findings to the wider scientific community, incorporating your key messages, successfully introducing your medicinal product to a welcoming market.

Our experienced med comms writers can help you with your product launch goals through strategic publication planning (whilst adhering to good publication planning practice 3 [GPP3] guidelines), and creation of a range of medical communications documents including:

  • Manuscripts (clinical studies, meta-analyses, reviews, surveillance studies)
  • Medical and scientific literature searches and reviews
  • Publication planning
  • Editorial support
  • Journal/conference submissions
  • Journal articles
  • Abstracts
  • Posters
  • Powerpoint slide presentations and kits
  • Summary of product characteristics
  • Patient information leaflets
  • Monographs
  • Formulary packs
  • White papers
  • Digital content (website copy, blogs, newsletters, press releases)
  • Advisory board agenda and reports
  • Conference articles, reports, and transcripts

Get in touch to learn how we can help you!